Qure.Ai Technologies Pvt. , Ltd. is one of 127 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Qure.Ai Technologies Pvt. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: qCT Lung (v1.0)
1
Total
1
Cleared
0
Denied
Qure.Ai Technologies Pvt. , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Mumbai, IN.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Qure.Ai Technologies Pvt. , Ltd. Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Qure.Ai Technologies Pvt. , Ltd.
1 devices